Journal
ORGANOMETALLICS
Volume 26, Issue 9, Pages 2228-2233Publisher
AMER CHEMICAL SOC
DOI: 10.1021/om070087y
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Catalytic amounts (1-0.1 mol %) of nickel and platinum compounds in 0, I, and II oxidation states containing mono- and diphosphines ligands, in conjunction with alkyl Grignard reagents, promoted the desulfurization of dibenzothiophene (DBT), 4-methyldibenzothiophene (4-MeDBT), and 4,6-dimethyldibenzothiophene (4,6-Me2DBT), to produce the corresponding substituted and unsubstituted biphenyls. It was also observed that the use of polar solvents such as THF yielded thiols, while the use of nonpolar solvents allowed the complete desulfurization of these substrates.
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